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991.
992.
Novel lanthanide coordination compounds with ciprofloxacin (CPFX), including eleven complexes Ln(CPFX)2Cl(H2O), (Ln=Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb; n = 7, 8, 9) and crystalline [Ce(CPFX)2 (H2O)4] Cl (H2O)3.25 (C2H5‐OH)0.25, were synthesized. The crystal is of triclinic space group Pi with a= 1.3865(2) nm, b = 1.3899(3) nm, c = 1.6505(2) nm, a = 92.73(1)°, β= 114.39(1)°, γ=115.55 (1)°, Z = 2 and R = 0.0449. FT‐IR, electronic spectroscopy and X‐ray diffraction were employed to show that the lanthanide ion, which displays an eight‐coordinate structure, is chelated by 3‐carboxyl and 4‐keto oxygen donors of CPFX and two six‐membered chelate rings are formed. Test of in vitro antibacterial activity against E. coli, P. aeruginosa and S. aureus indicated that the in vitro antibacterial activity of the ligand can be improved by complexation with Ce(III). 相似文献
993.
Thestudiesofpolymersolutionpropertiesfromdilatetoconcentratedsolutionbyfluorescencetechniquehaveattractedmoreattentionsinrecentdecadesl'2.InordertoinvestigateintrachainandinterchainilltCractionsindilutesolutionregion,pyrenewasusedaslabelsattachedtopolystyrene,whichwasintenselyfluorescentwithalongfluorescentlifetime3.Inthepresentwork,thepolystyreneattachedwithpyrenylgroupshadanunfavourablestrUcturetothenearestneighborexcimerformationwiththepyrenylgroupsseparatedbymorethanthreeatomsalongthechain… 相似文献
994.
SinceTangetaldevelopedanoveltWo-layerorganicelectr0luminescentdevice(OELD)inl987successfully',OELDhasattractedmuchinterestall0verthew0rId.ltisregardedas"havingbr0ughtthethirdrev0luti0ntoflatpaneldisplay"',becauseithass0manyadvantagessuperiort0CathodeRayTube(CRT)andLiquidCrystalDevice(LCD).Ithasl0wdrivenvoltage(lO0,000cd/m=),highluminescentefficiency(l5lIn/w),goodstability(50,000h),andithassimplestructureandiseasytofabricate'.ComparedtoinorganicELD,OELDiseasie… 相似文献
995.
Patrick Marks Sage Cohen Mindy Levine 《Journal of polymer science. Part A, Polymer chemistry》2013,51(19):4150-4155
Reported herein is the highly efficient quenching of fluorescent organic nanoparticles by 2,4‐dinitrotoluene and 2,4,6‐trinitrotoluene. These fluorescent nanoparticles are formed from the hydrophobic collapse of fluorescent polymer chains and display quenching efficiencies that are in line with the highest reported literature values. Moreover, the fluorescent quenching occurs only for the fluorescent nanoparticles, and not for the precursor polymer solutions, which display marked insensitivity to the presence of nitroaromatics. This aggregation‐dependent fluorescent quenching has numerous applications for the detection of small‐molecule electron‐deficient analytes. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2013 , 51, 4150–4155 相似文献
996.
Ying Lin Zhi‐Kuan Chen Teng‐Ling Ye Yan‐Feng Dai Dong‐Ge Ma Zhun Ma Qin‐De Liu Yu Chen 《Journal of polymer science. Part A, Polymer chemistry》2010,48(2):292-301
A series of conjugated blue‐light‐emitting copolymers, PTC‐1 , PTC‐2 , and PTC‐3, comprised different ratios of electron‐withdrawing segments (spirobifluorene substituted with cyanophenyl groups) and electron‐donating segments (tricarbazole‐triphenylamines), has been synthesized. The structures of these polymers were characterized and their thermal, photophysical, electrochemical, and electroluminescence properties were measured. Incorporation of rigid spirobifluorene units into the copolymers led to blue‐shifted absorption peaks in dilute toluene solution. Cyclic voltammetric measurement indicated the bandgaps of the polymers were in the range of 2.77–2.94 eV. It was found that increasing cyanophenyl‐spirobifluorene content in the polymer backbone lowered both the HOMO and LUMO energy levels of the copolymers, which was beneficial for electron injection/transporting in the polymer layer of the device. OLED device evaluation indicated that all the polymers emitted sky blue to deep blue light when the pure polymers were used as the emissive layers in the devices with a configuration of ITO/PEDOT:PSS/polymers/CsF/Ca/Al. The devices have been optimized by doping 30 wt % PBD into the polymer layers. Among the doped devices, PTC‐2 showed the best performance with the turn‐on voltage of 3.0 V, maximum brightness of 7257 cd/m2, maximum current efficiency of 1.76 cd/A, and CIE coordinates of (0.15, 0.14). © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 292–301, 2010 相似文献
997.
C. Fitzpatrick E. Lewis A. Al-Shamma’a I. Pandithas J. Cullen J. Lucas 《Optical Review》2001,8(6):459-462
Low-pressure mercury lamps are commonly used for germicidal applications such as water and wastewater sterilisation. The germicidal
effect is due to the emission of light at 254 nm, which leads to the destruction of most waterborne bacteria. The Microwave
plasma ultraviolet lamp (MPUVL) is a new technology for generating a high intensity ultraviolet (UV) light. A Fluorescent
optical fiber based sensor is presented which is used for monitoring the output of a high power microwave UV light source
and its control. This sensor is a fiber which has had its cladding removed and been coated with a phosphor doped polymer.
This paper was originally presented at the 2001 International Conference (2nd Joint OSJ-SPIE Conference) on Optical Engineering
for Sensing and Nanotechnology, ICOSN 2001 which was held June 6–8, 2001 at the Pacifico-Yokohama Conference Center, Yokohama,
Japan. 相似文献
998.
Chemometric methods like principal component regression (PCR) are an excellent tool for the determination of matrix parameters from scattered radiation. PCR is used for the determination of carbon, hydrogen and oxygen from water and oil-based samples. This information is used in combination with fundamental parameters to determine zink in liquid samples. The method allows an accurate prediction of element concentrations in strong varying matrices. 相似文献
999.
Hiroyuki Okamura Hiroki SakaeKeiji Kidani Naoki HirayamaNoboru Aoyagi Takumi SaitoKojiro Shimojo Hirochika NaganawaHisanori Imura 《Polyhedron》2012,31(1):748-753
The extraction constant and the two-phase stability constant (KD,Mβ3) of tris(2-thenoyltrifluoroacetonato)europium(III) between 1-butyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide ([C4mim][Tf2N]) as an ionic liquid and an aqueous phase were determined by considering the extraction equilibria including anionic tetrakis(2-thenoyltrifluoroacetonato)europate(III). Specific solute-solvent interactions between the neutral Eu(III) chelate and [C4mim][Tf2N] molecules were revealed from the relationships between the distribution constant of the enol form of 2-thenoyltrifluoroacetone (Htta) as a proton chelate and the distribution constant (KD,M) of the neutral Eu(III) chelate because the [C4mim][Tf2N] system gave the high KD,Mβ3 value compared with those in conventional molecular solvents such as benzene and 1,2-dichloroethane. The coordination environment of Eu3+ in the neutral Eu(III) chelate in [C4mim][Tf2N] was investigated by time-resolved laser-induced fluorescence spectroscopy and infrared absorption spectroscopy. Both methods consistently indicated that not only the Eu(III) chelate extracted but also Eu(tta)3(H2O)3 synthesized as a solid crystal were almost completely dehydrated in [C4mim][Tf2N] saturated with water. Consequently, the higher KD,M or extractability of the neutral Eu(III) chelate in the [C4mim][Tf2N] system can be ascribed to the dehydration of the Eu(III) chelate, which is caused by the specific solvation with [C4mim][Tf2N] molecules. 相似文献
1000.
Javier Gallego David Prez‐Foullerat Francisco Mendicuti Wayne L. Mattice 《Journal of Polymer Science.Polymer Physics》2001,39(12):1272-1281
The ratios of the intensity of excimer and monomer emissions, denoted IE/IM, in poly(N‐vinyl carbazole) and copolymers of N‐vinyl carbazole and methyl methacrylate were measured with steady‐state fluorescence. Measurements were performed in dilute solutions of several fluid solvents at 25 °C and in a solid matrix of poly(methyl methacrylate) at room temperature. The values of IE/IM depended on the nature of the solvent, the emission wavelength, and the copolymer composition. Molecular dynamics simulations were performed for diastereoisomers of 2,4‐di(N‐carbazolyl)pentane and for isotactic and syndiotactic trichromophoric copolymer fragments to assist in the identification of the thermally accessible conformations capable of forming intramolecular excimers and the configurational relationship of the carbazole units in these complexes. Nearest neighbor carbazole groups made the dominant contribution to the excimers. Excimers were more likely in isotactic sequences than in syndiotactic sequences, as was also the case for the low‐energy excimer arising from the complete overlap of two carbazole units. © 2001 John Wiley & Sons, Inc. J Polym Sci Part B: Polym Phys 39: 1272–1281, 2001 相似文献